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What Phase 2 is not powered to do is detect rarer adverse events, confirm long-term safety, or establish outcomes over years of use

All procedures were performed within laminar flow cabinets to reduce the risk of airborne microplastic contamination

All study participants were randomly assigned to an experimental treatment group that received subcutaneous injection of cagrilintide, once-weekly, in doses of either 0.3, 0.6, 1.2, 2.4, or 4.5 mg, as well as a one-daily 3.0 mg dose of liraglutide, and a volume matched placebo for control purposes

And sometimes they can be blinded by a goal. Of course, as we now know, this was no small breakdown